Variant #0000973854 (NC_000001.10:g.247835961T>C, NM_012353.2:c.*84803A>G (OR1C1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.247835961T>C
DNA change (hg38) -
Published as OR13G1(NM_001005487.2):c.383A>G (p.(His128Arg))
ISCN -
DB-ID OR1C1_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00345 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR11L1 NM_001001959.1 -?/. - c.*168269A>G r.(=) p.(=)
OR14A16 NM_001001966.1 -?/. - c.*142141A>G r.(=) p.(=)
OR6F1 NM_001005286.1 -?/. - c.*39170A>G r.(=) p.(=)
OR13G1 NM_001005487.1 -?/. - c.383A>G r.(?) p.(His128Arg)
OR1C1 NM_012353.2 -?/. - c.*84803A>G r.(=) p.(=)
TRIM58 NM_015431.3 -?/. - c.-184588T>C r.(?) p.(=)


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